Serve as a hands-on technical expert across SAP systems, actively engaging in ABAP programming, Fiori app development, SAP Basis administration, and SAP Security roles and authorizations
Participate in design, development, debugging, performance tuning, and deployment activities to ensure stable, secure, and scalable solutions
Develop and maintain a comprehensive technical blueprint for GMP systems, aligning technology services with business objectives and regulatory requirements
Provide architectural leadership in resolving inter-program and inter-project issues related to GMP systems
Partner with the IDMO Business to develop and execute against an IT roadmap and deliver on the IT infrastructure needed to manufacture autologous and allogeneic cell therapy products
Work closely with Validation and Quality in deploying and supporting IT GMP Systems
Manage and coordinate employees, contractors, and agencies involved in development projects to ensure alignment with project goals, timelines, budgets, and quality standards
Establish KPIs, monitor progress, and keep critical stakeholders informed of progress for IT projects and strategic initiatives
Establish key stakeholder relationships with internal and external stakeholders
Work closely with other functional areas to develop and execute against the strategic plan for all Cellares sites
Serve as a subject matter expert (SME) during audits or inspections by regulatory authorities
Requirements
Bachelor’s degree in Computer Science or a related technical field
Minimum of 10+ years of experience within IT in a cGMP environment in the biotech/biopharma industry, including at least 5 years of leadership or lead developer experience
Strong, hands-on experience in SAP development, including ABAP programming, Fiori/UI5 app development, and related SAP technology stacks
Experience in interface development and management using platforms such as MuleSoft, Workato, or similar integration tools
Experience implementing and supporting Manufacturing, Quality, and Supply Chain applications, including ERP, MES, LIMS, QMS, etc.
Ability to manage shifting priorities to meet critical deadlines in a fast-paced and dynamic environment while maintaining clarity of focus
Proven ability to deliver results independently with a proactive, hands-on approach to technical problem solving
Demonstrated success in building scalable, compliant, and supportable GMP systems with minimal supervision
Strong analytical and critical thinking skills with a detail-oriented mindset
Excellent teamwork and interpersonal skills; ability to communicate technical concepts to non-technical stakeholders
Strong written and verbal communication skills
Self-motivated with a passion for technology and continuous learning
Self-awareness, integrity, authenticity, and a growth mindset
Benefits
competitive base salaries
highly subsidized Medical, Dental, and Vision Plans
401(k) Matching
Free EV Charging
Onsite lunches
Stock options
All displayed pay ranges are approximate, negotiable, and location dependent.
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